A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038030



Internal ID19127249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26861..98907hg38UCSC Ensembl
Innerchr10:72797..144847hg19UCSC Ensembl
Innerchr10:62797..134847hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3872047
hg1972051
hg1872051
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv647n100
Supporting Variantsnssv3486797, nssv3498991, nssv3484985, nssv3495219, nssv3492482, nssv3484889, nssv3486997, nssv3490586, nssv3489074, nssv3492778, nssv3493056, nssv3489605, nssv3485435, nssv3483134, nssv3496718, nssv3498044, nssv3499160, nssv3500527
Samples
Known GenesTUBB8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038030
Frequency
Sample Size11257
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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